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rs796053008

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053008(A;A)
Make rs796053008(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165999776
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053008
ebirs796053008
HLIrs796053008
Exacrs796053008
Varsomers796053008
Maprs796053008
PheGenIrs796053008
hapmaprs796053008
1000 genomesrs796053008
hgdprs796053008
ensemblrs796053008
gopubmedrs796053008
geneviewrs796053008
scholarrs796053008
googlers796053008
pharmgkbrs796053008
gwascentralrs796053008
openSNPrs796053008
23andMers796053008
23andMe allrs796053008
SNP Nexus

SNPshotrs796053008
SNPdbers796053008
MSV3drs796053008
GWAS Ctlgrs796053008
Max Magnitude0
ClinVar
Risk rs796053008(A;A)
Alt rs796053008(A;A)
Reference rs796053008(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166856286C>T
CLNSRC
CLNACC RCV000188945.2,